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101.
Human β-glucuronidase: Assignment of the structural gene to chromosome 7 using somatic cell hybrids 总被引:1,自引:0,他引:1
P. A. Lalley J. A. Brown R. L. Eddy L. L. Haley M. G. Byers A. P. Goggin T. B. Shows 《Biochemical genetics》1977,15(3-4):367-382
-Glucuronidase (GUS) has become an important enzyme model for the genetic study of molecular disease, enzyme realization, and therapy, and for the biogenesis and function of the lysosome and lysosomal enzymes. The genetics of human -glucuronidase was investigated utilizing 188 primary man-mouse and man-Chinese hamster somatic cell hybrids segregating human chromosomes. Cell hybrids were derived from 16 different fusion experiments involving cells from ten different and unrelated individuals and six different rodent cell lines. The genetic relationship of GUS to 28 enzyme markers representing 19 linkage groups was determined, and chromosome studies on selected cell hybrids were performed. The evidence indicates that the -glucuronidase gene is assigned to chromosome 7 in man. Comparative linkage data in man and mouse indicate that the structural gene GUS is located in a region on chromosome 7 that has remained conserved during evolution. Involvement of other chromosomes whose genes may be important in the final expression of GUS was not observed. A tetrameric structure of human -glucuronidase was demonstrated by the formation of three heteropolymers migrating between the human and mouse molecular forms in chromosome 7 positive cell hybrids. Linkage of GUS to other lysosomal enzyme genes was investigated. -Hexosaminidase HEX
B) was assigned to chromosome 5; acid phosphatase2
(ACP
2) and esterase A4
(ES-A
4) were assigned to chromosome 11; HEX
A was not linked to GUS; and -galactosidase (-GAL) was localized on the X chromosome. These assignments are consistent with previous reports. Evidence was not obtained for a cluster of lysosomal enzyme structural genes. In demonstrating that GUS was not assigned to chromosome 9 utilizing an X/9 translocation segregating in cell hybrids, the gene coding for human adenylate kinase1 was confirmed to be located on chromosome 9.Supported by NIH Grants HD 05196, GM 20454, and GM 06321, by NSF Grant BMS 73-07072, and by HEW Maternal and Child Health Service, Project 417. 相似文献
102.
J. J. González-Aguilera A. Ma. Fernández-Peralta 《Plant Systematics and Evolution》1981,139(1-2):147-154
The meiotic behaviour abnormalities, fertility and size of pollen of 6 taxa ofSesamoides have been analysed. Besides diploids (2x), polyploids (4x, 6x, 8x) have been found. The chromosome base number is x = 10, but an origin from x = 5 is suggested. 相似文献
103.
E. Jacobsen 《Plant Cell, Tissue and Organ Culture》1981,1(1):77-84
Cytological studies on leaf callus cells and regenerated potato plants suggest that it may be possible to utilize somatic
chromosome doubling to obtain tetraploids from outstanding dihaploid breeding clones. The ploidy levels found in callus-derived
plants were diploid, tetraploid, and octaploid, but the proportion of these was dependent on the donor genotype. L1 and L3 germ layers were studied in more than 300 plants; periclinal ploidy chimerism, an undesirable feature of colchicine doubling,
was not found.
Leaf callus was more efficiently induced using NAA than 2, 4-D as an auxin source in the Murashige and Skoog medium. A high
proportion of dividing cells in young calli were polyploid. The frequency of doubled and octaploid plants regenerated was
significantly dependent on donor genotype. The extent of polyploidization was marginally higher after callus growth on a medium
containing 2, 4-D than in a medium containing NAA. In some genotypes the chromosome numbers of regenerated plants were variable,
being less than tetraploid (mixohypotetraploid). After tuber propagation, the original ploidy level was maintained although
mixohypotetraploidy persisted.
In a few somatically doubled clones, male fertility was tested and found to be satisfactory with respect to seed-setting. 相似文献
104.
M. Anastassova-Kristeva H. Nicoloff S. Georgiev 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1978,53(5):229-231
Summary Six varieties of Triticum monococcum were analysed by means of the nucleolar test; i.e., estimation of the maximum number of primary nucleoli per nucleus. All of the varieties exhibited 4 primary nucleoli in telophase and early interphase. Following detailed karyological analysis four SAT chromosomes in all six karyotypes were found in accordance with the maximum nucleolar number. Secondary constrictions and microsatellites were localised on the short arms of chromosome pairs 3 and 5. A new order of the chromosomes in the idiogram of Tr. monococcum is proposed. 相似文献
105.
Ram S. Verma Carole Rubenstein Harvey Dosik 《In vitro cellular & developmental biology. Plant》1977,13(11):806-807
Summary There was no significant difference in the mitotic indices of the cultures maintained at different CO2 concentrations, i.e. 0%, 5% and 10%. However, considerable variation was recorded among different individuals.
Supported by National Cancer Institute Contract No. 1 CP 43251. 相似文献
106.
Electrophoretic variation characterized by the presence (ES-5B+) or absence (ES-5B–) of esterase-5B in the plasma of the house mouse has been observed. It is suggested that the expression of esterase-5B is controlled by an autosomal locus, Esr, linked to Ldr-1 on chromosome 6, in addition to the presumptive structural locus Es-5, which is located on chromosome 8. A gene order of Lyt-3-Esr-Ldr-1 was determined by two crosses.Supported by the Deutsche Forschungsgemeinschaft (SFB 46).This is communication No. 33 of a research program devoted to the investigation of cellular distribution and genetics of nonspecific esterases. 相似文献
107.
The contributions of each chromosome to the traits thorax size and plasticity of thorax size as affected by temperature in Drosophila melanogaster were measured. A composite stock was created from lines previously subjected to selection on thorax size or plasticity of thorax size. A chromosome extraction was performed against a uniform background lacking genetic variation, provided by a stock of marked balancer flies. With regard to amount of plasticity, chromosome I and the balancer stock showed no plasticity, the composite stock showed the greatest plasticity, and chromosomes II and III were intermediate. Chromosome I showed significant genetic variation for thorax size at both 19° C and 25° C, but not for plasticity, while chromosome II showed significant genetic variation for plasticity, but not for thorax size. Chromosome III showed significant genetic variation for both thorax size and plasticity. We tested the predictions of three models of the genetic basis of phenotypic plasticity: overdominance, pleiotropy, and epistasis. The results support the epistasis model, in agreement with earlier work. The amount of developmental noise was correlated with phenotypic plasticity at 25° C, in agreement with earlier work. A negative correlation was found at 19° C for chromosome II, contrary to earlier work. 相似文献
108.
A case of somatic instability affecting aleurone colour in a strain of maize from India with flint background was analysed.
The somatic instability is localized to theC
1 (Inhibitor) allele ofC locus on the short arm of chromosome 9. Molecular tests indicated thatAc is not present in the Indian stock and the evidence is consistent with the involvement of theEn (Spm) transposable element in the instability. The presence of theEn (Spm)-like element in the stock would suggest that these elements have been present in the maize genome for a long time. A new
allele ofshrunken (sh1) gene with a somewhat unorthodox breeding behaviour is also described. 相似文献
109.
Spermatogenesis in XY, XYSxra and XOSxra mice: a quantitative analysis of spermatogenesis throughout puberty 总被引:1,自引:0,他引:1
Adult XYSxra mice exhibit varying degrees of spermatogenic deficiency but are usually fertile, while XOSxra mice have severe spermatogenic failure and are always sterile. The present quantitative spermatogenic analysis documents when these anomalies first appear during puberty. The results demonstrate that in XYSxra mice there was increased degeneration of pachytene spermatocytes and, to a lesser extent, meiotic metaphase stages. On average, there were only one-half the number of spermatids compared with the XY controls. The defect in XOSxra mice appeared a little later, with an almost complete arrest and degeneration during the meiotic metaphases, so that the number of spermatids produced was only 3% of the control value. These results are discussed in relation to an hypothesis that links sex chromosome univalence during meiotic prophase with spermatogenic failure. 相似文献
110.
Flow cytometry and plant protoplast cell biology 总被引:3,自引:0,他引:3